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1.
Artículo en Inglés | IMSEAR | ID: sea-153786

RESUMEN

Wide spread use of Di-(2-ethylhexyl) phthalate (DEHP) has made it a ubiquitous contaminant in today’s environment, responsible for possible carcinogenic and endocrine disrupting effects. In the present investigation an integrative toxico-proteomic approach was made to study the estrogenic potential of DEHP. In vitro experiments carried out with DEHP (0.1-100 μM) induced proliferations (E-screen assay) in human estrogen receptors-α (ERα) positive MCF-7 and ERα negative MDA-MB-231 breast cancer cells irrespective of their ERα status. Further, DEHP suppressed tamoxifen (a potent anti-breast cancer drug) induced apoptosis in both cell types as shown by flowcytometric cell cycle analysis. Label-free quantitative proteomics analysis of the cell secretome of both the cell lines indicated a wide array of stress related, structural and receptor binding proteins that were affected due to DEHP exposure. The secretome of DEHP treated MCF-7 cells revealed the down regulation of lactotransferrin, an ERα responsive iron transport protein. The results indicated that toxicological effects of DEHP did not follow an ERα signaling pathway. However, the differential effects in MCF-7 and MDA-MB-231 cell lines indicate that ERα might have an indirect modulating effect on DEHP induced toxicity.


Asunto(s)
Apoptosis/efectos de los fármacos , Neoplasias de la Mama/patología , Ciclo Celular/efectos de los fármacos , División Celular/efectos de los fármacos , Línea Celular Tumoral/efectos de los fármacos , Línea Celular Tumoral/metabolismo , Dietilhexil Ftalato/toxicidad , Contaminantes Ambientales/toxicidad , Receptor alfa de Estrógeno/efectos de los fármacos , Receptor alfa de Estrógeno/fisiología , Estrógenos , Femenino , Regulación Neoplásica de la Expresión Génica/efectos de los fármacos , Humanos , Lactoferrina/biosíntesis , Lactoferrina/genética , Lactoferrina/metabolismo , Células MCF-7/efectos de los fármacos , Células MCF-7/metabolismo , Espectrometría de Masas/instrumentación , Microquímica/instrumentación , Proteínas de Neoplasias/efectos de los fármacos , Proteínas de Neoplasias/fisiología , Proteínas de Neoplasias/metabolismo , Neoplasias Hormono-Dependientes/patología , Proteómica , Tamoxifeno/antagonistas & inhibidores , Tamoxifeno/farmacología
2.
J. appl. oral sci ; 18(2): 166-170, Mar.-Apr. 2010. ilus, tab
Artículo en Inglés | LILACS | ID: lil-550408

RESUMEN

OBJECTIVE: The present study evaluated the association between lactotransferrin (LTF) gene polymorphism (exon 2, A/G, Lys/Arg) and dental caries. MATERIAL AND METHODS: A convenience sample of 110 individuals, 12 years old, was divided into: group 1, 48 individuals without caries experience (DMFT=0), and group 2, 62 subjects with caries experience (DMFT>1). DNA was obtained from a mouthwash with 3 percent glucose solution, followed by a scrapping of the oral mucosa. After DNA purification, polymerase chain reaction (PCR), single strand conformation polymorphism (SSCP) was performed to access the study polymorphism. The LTF A/G (Lys/Arg) polymorphism had been previously reported as located in exon 1. RESULTS: Allele 1 of the study polymorphism was associated with low DMFT index and showed a protective effect against caries experience (OR=0.16, IC=0.03-0.76, p=0.01). CONCLUSIONS: Lactotransferrin A/G (exon 2, Lys/Arg) polymorphism was associated with susceptibility to dental caries in 12-year-old students.


Asunto(s)
Niño , Humanos , Susceptibilidad a Caries Dentarias/genética , Caries Dental/genética , Lactoferrina/genética , Alelos , Sustitución de Aminoácidos , Arginina , Secuencia de Bases , Estudios de Casos y Controles , Índice CPO , Análisis Mutacional de ADN , Frecuencia de los Genes , Lisina , Datos de Secuencia Molecular , Polimorfismo de Nucleótido Simple , Polimorfismo Conformacional Retorcido-Simple , Saliva
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